6647-96-7 Usage
Uses
Used in Organic Synthesis:
MFCD15146432 is used as a reagent in organic synthesis reactions for various applications, including the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Its versatility as a reagent allows for the synthesis of a wide range of compounds with diverse functional groups and structural features.
Used in Research and Development:
MFCD15146432 is utilized in research and development laboratories for the study of chemical reactions, mechanisms, and the development of new synthetic methodologies. Its unique properties and reactivity make it a valuable tool for chemists working on innovative approaches to chemical synthesis.
Used in Quality Control and Analysis:
MFCD15146432 can be employed as a reference compound in quality control and analysis processes to ensure the purity and consistency of synthesized products. Its well-defined chemical structure and properties make it suitable for use as a benchmark in analytical methods.
Used in Education and Training:
MFCD15146432 serves as an educational tool in academic and training settings, where it can be used to demonstrate the principles of organic synthesis, reaction mechanisms, and the handling of hazardous substances. Its sensitivity to heat, light, and air also provides an opportunity to teach proper laboratory safety practices.
Check Digit Verification of cas no
The CAS Registry Mumber 6647-96-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,4 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6647-96:
(6*6)+(5*6)+(4*4)+(3*7)+(2*9)+(1*6)=127
127 % 10 = 7
So 6647-96-7 is a valid CAS Registry Number.
6647-96-7Relevant academic research and scientific papers
2 - Alkynyl mannose derivative and application thereof
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Paragraph 0082-0084, (2021/10/05)
The present invention relates to a 2-alkynyl mannose derivative and an application thereof. The mannose derivative, as well as a pharmaceutically acceptable salt, an isotope and an isomer thereof have the structure represented by general formula I. The de
HETEROARYLPHENOXY BENZAMIDE KAPPA OPIOID LIGANDS
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Paragraph 0283; 0284, (2018/06/09)
The present invention provides compounds of Formula I: and pharmaceutically acceptable salts thereof wherein the variables R1, R2, R3, R4, R9, X, m and n are as defined herein; processes for the prepa
Two-stage sonogashira coupling method in the synthesis of auxin active acetylenes
Wayne Craig,Eberle, Martin,Irminger, Bruno,Schueckenboehmer, Anegret,Laime, Yvette,Mueller, Patrick
, p. 1967 - 1974 (2008/09/16)
A sequential Sonogashira coupling of a protected acetylene precursor with aryl halides (5) followed by pyrazolyl iodides (14) allows efficient access to the unsymmetrical aryl-heteroarylacetylene (8). Subsequent regioselective lithiation exchange followed by dimethyl oxalate quench produced readily vicinal ketoesters (9) which show auxin effects in a wide variety of plant species.
